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AS703026

Chemical Structure : AS703026

CAS No.: 1236699-92-5

AS703026 (Pimasertib;MSC1936369B;AS-703026;AS 703026)

Catalog No.: PC-42857Not For Human Use, Lab Use Only.

AS703026 (Pimasertib, MSC1936369B) is a potent, selective, allosteric, orally bioavailable MEK1/2 inhibitor, inhibits the growth of MM cell lines with IC50 of 0.005-2 uM.

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25 mg $98 In stock
100 mg $248 In stock
200 mg $388 In stock
1 g $388 In stock

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Purity & Documentation Purity: >98% (HPLC) Select Batch:

Biological Activity

AS703026 (Pimasertib, MSC1936369B) is a potent, selective, allosteric, orally bioavailable MEK1/2 inhibitor, inhibits the growth of MM cell lines with IC50 of 0.005-2 uM.
AS703026 (Pimasertib) has IC50 of 10 nM against INA-6 cells, approximately 10-fold more potent than AZD6244 at inhibiting cytokine-induced osteoclast differentiation in vitro.
AS703026 (Pimasertib) effectively inhibits the growth of D-MUT cells in vitro and in vivo by specific inhibition of the key MEK downstream target kinase ERK.
AS703026 (Pimasertib) also enhances gemcitabine efficacy in pancreatic cancer models by reducing ribonucleotide reductase subunit-1 (RRM1).

Physicochemical Properties

M.Wt 431.2008
Formula C15H15FIN3O3
Appearance Solid
CAS No.
Storage
Solide Powder
-20 °C 12 Months; 4°C 6 Months
In Solvent
-80 °C 6 Months; -20°C 6 Months
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

4-Pyridinecarboxamide, N-[(2S)-2,3-dihydroxypropyl]-3-[(2-fluoro-4-iodophenyl)amino]-

References

1. Kim K, et al. Br J Haematol. 2010 May;149(4):537-49.

2. Yoon J, et al. Cancer Res. 2011 Jan 15;71(2):445-53.

3. Park SJ, et al. Am J Med Sci. 2013 Dec;346(6):494-8.

4. Vena F, et al. Clin Cancer Res. 2015 Dec 15;21(24):5563-77.

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